EnhancerAtlas 2.0: an updated resource with typical enhancer annotation in 600 tissue/cell types across nine species
EnhancerAtlas 2.0
TagContent
EnhancerAtlas ID
HS133-22319 
Organism
Homo sapiens 
Tissue/cell
melanoma 
Coordinate
chr3:50636620-50639290 
TF binding sites/motifs
Number: 4             
TFJASPAR IDCoordinateMotif SequenceStrand-Log10(p-value)
Stat6MA0520.1chr3:50638655-50638670CAGTTCCTGAGAAGC+6.51
ZIC1MA0696.1chr3:50637318-50637332GGCCCCCTGCTGTG+7.38
ZIC3MA0697.1chr3:50637318-50637333GGCCCCCTGCTGTGG+6.16
ZIC4MA0751.1chr3:50637318-50637333GGCCCCCTGCTGTGG+6.34
Number of super-enhancer constituents: 41             
IDCoordinateTissue/cell
SE_00760chr3:50636720-50645111Adipose_Nuclei
SE_09279chr3:50636789-50643770CD14
SE_12298chr3:50637567-50641454CD3
SE_12583chr3:50637855-50638154CD34_adult
SE_12583chr3:50638231-50638567CD34_adult
SE_12583chr3:50638834-50639286CD34_adult
SE_12919chr3:50637190-50639496CD34_Primary_RO01480
SE_13361chr3:50636482-50651600CD34_Primary_RO01536
SE_14184chr3:50637803-50641619CD34_Primary_RO01549
SE_14601chr3:50635365-50652110CD4_Memory_Primary_7pool
SE_15705chr3:50637773-50640862CD4_Memory_Primary_8pool
SE_16238chr3:50637562-50640385CD4_Naive_Primary_7pool
SE_16582chr3:50637829-50640336CD4_Naive_Primary_8pool
SE_17166chr3:50637926-50640703CD4p_CD225int_CD127p_Tmem
SE_18495chr3:50635603-50652144CD4p_CD25-_Il17-_PMAstim_Th
SE_19130chr3:50636430-50651976CD4p_CD25-_Il17p_PMAstim_Th17
SE_20626chr3:50637316-50651753CD56
SE_20911chr3:50636515-50652055CD8_Memory_7pool
SE_23649chr3:50636580-50642032Colon_Crypt_1
SE_23932chr3:50636606-50641027Colon_Crypt_2
SE_25135chr3:50636534-50641205Colon_Crypt_3
SE_25369chr3:50635253-50654453DND41
SE_26772chr3:50636910-50645175Esophagus
SE_27877chr3:50636977-50641548Fetal_Intestine
SE_28892chr3:50636927-50641567Fetal_Intestine_Large
SE_30531chr3:50636456-50641120Fetal_Muscle
SE_31573chr3:50636327-50646177Gastric
SE_40028chr3:50636324-50651737K562
SE_40824chr3:50635650-50651738Left_Ventricle
SE_42458chr3:50635760-50651762Lung
SE_47024chr3:50636967-50638655Ovary
SE_47024chr3:50638661-50639495Ovary
SE_47758chr3:50636646-50641285Pancreas
SE_48262chr3:50636469-50651773Psoas_Muscle
SE_49250chr3:50636324-50643972Right_Atrium
SE_49448chr3:50636552-50640884Right_Ventricle
SE_50378chr3:50636461-50651683Sigmoid_Colon
SE_51369chr3:50636562-50644163Skeletal_Muscle
SE_52764chr3:50636819-50646284Small_Intestine
SE_53704chr3:50636516-50641543Spleen
SE_65451chr3:50636456-50645477Pancreatic_islets
Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder
Number of disease enhancers: 4             
ChromosomeStartEnd
chr35063737850637476
chr35063699650637093
chr35063835350638905
chr35063698550637600
Enhancer Sequence
AGCCAGCCTG ACCTGGGTGC AGGCATCAAG GCCTCTAAGT GACAGAGAAT GCAGCACTCC 60
CACCCACTGC CAGCTGCCCC AGGTAGCTTC TGAGAACTGG CCACTGCAGA GTACAAGCAC 120
AGCAATGACC TGTGTCCTTG GGCTGCCCCA CTGCCCTCCT ACAGGGGAGG GAGGACCTCT 180
CTGCCATAGC CCCACCTCAC AGCTGCCACC CACCCACTGG GTCCTAGCCC TTCTTAACGC 240
CAGCATTGTC CCCATCTTCT CTGTGACATT GGGGTGGATG GGTAGCACGC TTGGCGCTGT 300
GCTCAGTGAG GGCCAAGGAG TGACCTGAGG GTGGGAGGAG AGAGGCAAGT TCTTGCCGAC 360
ACCCCGTCCA GCCTTGGCCA GGGGAGGTTC TCCATTCTGA AGGTAAAGGG GTCATGAGTG 420
GTTAAAAGGT TGTCCTAGTG CCTCCCAGCT ATGTGACCCT GACCTGCTCA CTCAGCACCC 480
TCAGCCATAC TTCCAGGCCC CTGCTCTAAC AATGCTGCTC CTGGGATCCT GTGATGGGAA 540
CACTCATGGC CATTCCCTTG AAATGTGGCC AGACTTCAAC CCAGTCCCAG ACAGTTGTCA 600
GTGCCCACTC ACTGCAGCCT CTCCTCTGCA TTCTCCAGGC TATTTTCCAA AAGGCCAGAT 660
GCATGTCCTG GGTGGCTTGA TGCTGAAGCT GGGGCCTGGG CCCCCTGCTG TGGGACAGGG 720
AAGTGTGGGT GAGACAAGGC TGTCCTGAAG GAGTGACTAG AGCCAGAGGC TGCCCACCAG 780
CAAAGGGGGC TCAGTGAGCA GGGCCTGGCA CTGCTGACCC CACCTTGTTT TCCCTCCTAC 840
TCTCCCTTGG TGCTTCACAC CCCCGGCTGC TCACTGGCCT AGGCAGGACA CTCCTGTCTA 900
ACCTCCTGCT TTCACTGTGG ACCCACACCC ACACGCTGCC TCCATAGGTA CACATGCCCT 960
TTTTTTCTCT ACTAACACCT GTTTCTCGTC GTCCACTCTG CCAGGCTGGA CACCGGGCAC 1020
TTCAGAGGTC ATGCCAGATC CAGCACCGGG ATGGAGGAGT CTAAGGAGGC ACCTGCAGTC 1080
AGGGAGGGCT TCCTGGAGGC AGAGACCGAA GCTAAGGGCT CAGTACCCTC TCCCCCCACT 1140
TACCCCAGGT CACTGGCTGT CCTCTGAGCC TCACTCCCTG GAAGGGCCAG CAGGTTCCAG 1200
GAAGTGTCCC CTCGCCCTGC AGTGCTGGTT CCAAGAACTG CAGCTCTTGG CAGCATTTGC 1260
TTAGGATCCT TTCCTAGAAC TTGAGACCTG CTCTGCCCAG ACTGCTGGGG TCTCAGAGGG 1320
CAGCCAGTGG GGGTAGTGGG GGAAGGGGGT GCACTGGGAG GTGCCTCTGC AGGTAGAACA 1380
TTCCATGGAC CAAACATTGG GAGGTGGGCC TAGGCTGTCA GCCGGGAGTG GTTGGCCACA 1440
CTAGGGTGGT CAACACCTCC AACAGGAGGT CGGTGAAATG CAGGTGCTTT GACTGCAGTC 1500
AACCATGGGG TGCGGGCCCA TGAGTTCTCC CTGCACAAGA AGGAGGCTCA TTCCCTTGGT 1560
CCAGAACTTC CACCAGCTTG CCACATGCCA CCCTCCACCC CCCGACTCTA CTCCCCCCAC 1620
TAGCCTGGCA CCAGGGTCCC ATCCCATAGA GAATCAGCAC AGGCCTTACC CTCAGAATAG 1680
GCCCTCATCA GATAACCTCC AGAGGACAGG CCAGGGTGCA GGACAGGCAG GTTCTGAGCA 1740
GGGAAGGGGG ATGGGATCGT CTTGGGGCCC TTGGAAGGCC ATGACACTTG TGTTATTAAT 1800
CCTGTTATAA TTTTACCTTT CCTGGTTAGA ACTGAATAAA TTACCCCACC TCACACCCCC 1860
CAGCAAAGTT GGGTCGGGTG AATGAGGGAC AGGCCCTGGT AAGTGGTCAA GGACAGGGCC 1920
CTACTTCCCT CAAGGTCACC AGGCCTCCCC CTGGGGCGTG TCCTCCACCC GCCACTTCTG 1980
AGCTGGCACC AGGCCTGCCC AGCCGCCTGG GACCTGCCAG ATCACGTTGA GCAACCAGTT 2040
CCTGAGAAGC GTTGAAGGCA GTGTGGTTTA AAATTAACTC CCCCGCTCCC CCTCCCGCCT 2100
GCGGCCTCCT CTGAGTTCTT GGAAGCGGCG CTCTGCTCTT CCTGGGAAGA GGCCTCCAGC 2160
CCCAGCTGCT GCAATTCTGG CGAAAACACC TCACCCAGGC TGGGGGTGGG GGGTGCCCAC 2220
GCCAGGCCTT CTCTGCCCTA CACAAGGCCC AGGGATCCTC TGGAAGCTAG CACCCACCCT 2280
AGTTACTCAC TGAGACCCAG AAGAGAAAGG GGGTGATTGT CAAGGTGCTG GGAGGAGGTG 2340
CTCCTGCCCC CAAAGCCCAC AGCTCCCAAC CAGGCACCTC TGGGTAGGAG AGAAAGTGAA 2400
TTGATCCCAC AACAGCAAAC CCAGGACCCT GGCCTACTTT GAGCCATATA TGTCCTGGCG 2460
AGATGCAGCA ACTTCCTAGG GCCACCCAGC TTTGCCTGCC CTTATAAGCT CAGCTTGCCC 2520
ACTAGGTGCC AGGCTGATGG TGCTGATCTG GCAAGGATGC CCGGGAGCAC GCCCCCGCAG 2580
GCATGCACAC ACCTGGGTTA ACAGTGATCT CTGCCAGGAT CTCTCCTTTT CTCTCACCCA 2640
CACCCCTCAA ACTGCCCTTG GAACACCTCT 2670